A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609014



Internal ID16049737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151065784..151128000hg38UCSC Ensembl
Innerchr7:150762871..150825087hg19UCSC Ensembl
Innerchr7:150393804..150456020hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3862217
hg1962217
hg1862217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11724n54
Supporting Variantsnssv1155701
Samples1780862416_A
Known GenesAGAP3, FASTK, SLC4A2, TMUB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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